Overexpression of Nrf2 attenuates Carmustine-induced cytotoxicity in U87MG human glioma cellsReport as inadecuate

Overexpression of Nrf2 attenuates Carmustine-induced cytotoxicity in U87MG human glioma cells - Download this document for free, or read online. Document in PDF available to download.

BMC Cancer

, 15:118

Cell and molecular biology


BackgroundMalignant glioma is one of the most devastating tumors in adults with poor patient prognosis. Notably, glioma often exhibits resistance to conventional chemotherapeutic approaches, complicating patient treatments. However, the molecular mediators involved in tumor chemoresistance remain poorly defined, creating a barrier to the successful management of glioma. In the present study, we hypothesized that the antioxidant transcription factor, Nrf2 nuclear factor erythroid-derived 2 like 2, attenuates glioma cytotoxicity to Carmustine BCNU, a widely used chemotherapeutic agent known to modulate cellular oxidative balance.

MethodsTo test the hypothesis, we employed human malignant glioma cell line, U87MG and overexpression of Nrf2 in glioma cells was achieved using both pharmacological and genetic approaches.

ResultsNotably, induction of Nrf2 was associated with increased expression of heme oxygenase-1 HO-1, a stress inducible enzyme involved in anti-oxidant defense. In addition, over expression of Nrf2 in U87MG cells significantly attenuated the cytotoxicity of Carmustine as evidenced by both cellular viability assay and flow cytometry analysis. Consistent with this, antioxidants such as glutathione and N-acetyl cysteine significantly reduced Carmustine mediated glioma cytotoxicity.

ConclusionsTaken together, these data strongly implicate an unexplored role of Nrf2 in glioma resistance to Carmustine and raise the possible use of Nrf2 inhibitors as adjunct to Carmustine for the treatment of malignant glioma.

KeywordsNrf2 Carmustine BCNU Glioma Chemotherapy Electronic supplementary materialThe online version of this article doi:10.1186-s12885-015-1134-z contains supplementary material, which is available to authorized users.

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Author: Sangeetha Sukumari-Ramesh - Niyathi Prasad - Cargill H AlleyneJr - John R Vender - Krishnan M Dhandapani

Source: https://link.springer.com/

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